A medical connector for use in a fluid pathway includes a substantially transparent housing having a proximal end with a proximal opening and a distal end with a distal opening, and a cavity extending therebetween. The connector provides a substantially visible fluid flow path extending through a substantial portion of the connector.

An implantable medical device configured to monitor fluid in proximity to an implantable medical device for an inadvertent introduction of infusate into a pocket of tissue surrounding the implantable medical device during a refill procedure, the implantable medical device including a refillable infusate delivery system, the refillable infusate delivery system including a reservoir in fluid communication with an access port, and a conductivity sensor configured to monitor fluid in proximity to the conductivity sensor for an introduction of infusate into a pocket of tissue surrounding the implantable medical device, wherein the conductivity sensor comprises a pair of electrodes positioned on an external surface of the implantable medical device.

A polymeric container for storing a drug such as insulin which comprises a hard shell (2) and a flexible film (1), wherein both elements are made from the same material.

A cosmic resonator is designed and constructed to trap the cosmic waves acting as a quantum trap the upper half of which is to absorb and the lower half is increase resonance and to increase the durability of input cosmic waves. The enhanced cosmic waves within the pyramid are used to load vitality force information on water or any water-based creature or matter with direct human exposure to cosmic waves and indirect gain with consumption of cosmic energetic products that are exposed to the waves to improve physical and mental health of humans.

An intravenous (IV) spike for administering a medicinal fluid from a container may include a head portion at a proximal end thereof, a base portion at a distal end thereof, and an elongate body portion connecting the head and the base portions. The elongate body portion may be configured to be coupled to the container. The IV spike may further include a radial notch extending at least partially along a circumference of an outer surface of the elongate body portion. The radial notch may be recessed radially inward from the outer surface.

A heating device for heating surgical tubes is disclosed herein. The heating device comprises a hollow housing configured to receive the surgical tubes therein. A heating element provided on the hollow housing. A first sensor is assembled on the heating element and configured to sense the temperature of the heating element. A controller is coupled to the heating element and the first sensor, wherein the controller is configured to receive an input associated with a required heating temperature from a user for heating the surgical tubes, and accordingly regulate the operation of the heating element based on the required heating temperature and an actual temperature sensed via the first sensor.

An intubation shield having a viewing panel and a front opening surrounded by a first side wall, a second side wall, a back wall and a front dome wall configured to cover at least a portion of the head, the neck and/or the upper torso of a patient to form a barrier between the covered parts of the patient and the upper body of the practitioner, wherein the viewing panel allows for uninterrupted visibility of an anatomical feature of the patient, and the front opening allows the body of the patient to be inserted while minimizing the droplet contamination, and a first arm hole on the first side wall and a second arm hole on the second side wall to increase the freedom of movement of the practitioner while performing medical procedures.

A CPAP system for respiratory therapy includes an RPT device configured to supply a flow of gas at a therapeutic pressure, a patient interface, an air delivery conduit configured to pass the flow of gas from the RPT device to the patient interface, and a vent assembly configured to provide a vent flow of gas to discharge gas exhaled by the patient from a pressurized volume to ambient. The vent assembly includes a base including at least one first orifice to allow gas to be discharged along a primary vent flow path and at least one second orifice to allow gas to be discharged along a secondary vent flow path, a diffusing member provided to the base, and a membrane provided to the base. The membrane is configured to apportion the vent flow of gas along the primary vent flow path and the secondary vent flow path throughout respiratory therapy.

A patient interface comprises a support structure and a seal-forming structure. The support structure is arranged to support the sealing portion and is configured to connect to the frame. The sealing portion comprises textile and is attached to the support structure along an outer perimeter of the sealing portion such that in use the sealing portion may be in tension due to reactive stress of the support structure and/or a resilient stretch characteristic of the textile such that the sealing portion exerts a force against the patient's face.

There is provided a dose counter assembly for use with a medicament dispenser, the dose counter assembly comprising: a) a units dose display means comprising a first count indicia and one or more driver teeth; b) a tens dose display means comprising a second count indicia; and c) a driver, wherein the first count indicia and second count indicia align at a common viewing area to collectively display a count sequence.